<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Benziane,A</style></author><author><style face="normal" font="default" size="100%">Kaci,L</style></author><author><style face="normal" font="default" size="100%">Missoum,S</style></author><author><style face="normal" font="default" size="100%">Lahmar,M</style></author><author><style face="normal" font="default" size="100%">Khellaf,G</style></author><author><style face="normal" font="default" size="100%">Benabadji,M</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Rapidly progressive renal failure to reveal LCAT deficiency in an Algerian family</style></title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://europepmc.org/article/MED/36420900</style></url></web-urls></urls><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Lecithin-cholesterol&amp;nbsp;acyltransferase (LCAT) deficiency is an autosomal recessive disorder that can reveal two different diseases: a very interesting nephrological picture of complete enzyme deficiency characterized by the association of dyslipidemia, corneal opacities, anemia, and progressive nephropathy; and a partial form (fish-eye disease) with dyslipidemia and progressive corneal opacities only. We report herein the case of a 35-year-old man&amp;nbsp;who presented hypertension, renal symptomatology of rapidly progressive glomerulonephritis associates: nephrotic proteinuria, severe renal failure, in combination with annular corneal opacities, anemia, and dyslipidemia. The diagnosis of familial LCAT deficiency was confirmed by clinical examination, characteristic dyslipidemia, undetectable LCAT levels in plasma, and positive family history.</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Boudouh,N</style></author><author><style face="normal" font="default" size="100%">Djebara,L</style></author><author><style face="normal" font="default" size="100%">Merdaci,N</style></author><author><style face="normal" font="default" size="100%">Mehdi,F</style></author><author><style face="normal" font="default" size="100%">Grainat;N</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">incidence de la douleur chronique post opératoire en chirurgie générale Journées Nationales de lutte contre la douleur SAETD</style></title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year></dates><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">KHANFRI,Y</style></author><author><style face="normal" font="default" size="100%">SEDFI</style></author><author><style face="normal" font="default" size="100%">hassinet</style></author><author><style face="normal" font="default" size="100%">Boudouh,N</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">anti mitochondries de type M2 chez l&amp;rsquo;enfant : à propos d&amp;rsquo;un cas</style></title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year></dates><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">DJARI,MH</style></author><author><style face="normal" font="default" size="100%">Boudouh,N</style></author><author><style face="normal" font="default" size="100%">Grainat,N</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Encéphalites :à propos d&amp;rsquo;un cas</style></title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year></dates><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">BAALOUDJ,N</style></author><author><style face="normal" font="default" size="100%">Boudouh,N</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Péridurale thoracique chez l&amp;rsquo;emphysémateux</style></title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year></dates><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Boudouh,N</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Douleur chronique post chirurgicale et cancer du sein</style></title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year></dates><language><style face="normal" font="default" size="100%">eng</style></language></record></records></xml>